Gene Details



FREM1 and homologs in 7 species are found in 565 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse MP 1087 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7747 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 386 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse MP 832 Genes GS166825: MP:0000462 abnormal digestive system morphology
Expand Tier I Human 63 Genes GS175327: HP:0000568 Microphthalmos
Expand Tier II Mouse 459 Genes GS129071: anticardiolipin antibody 2 (Acla2 Published QTL Chr 4)
Expand Tier I Mouse MP 85 Genes GS165857: MP:0000527 abnormal kidney development
Expand Tier II Human 1638 Genes GS236094: [MeSH] Scleroproteins : D012596
Expand Tier I Human GO 7611 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Human CTD 6060 Genes GS122891: Copper Sulfate interacting with Homo sapiens associated genes (MeSH:D019327) in CTD
Expand Tier I Mouse MP 51 Genes GS163317: MP:0000520 absent kidney
Expand Tier II Human 4818 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse MP 332 Genes GS168549: MP:0000477 abnormal intestine morphology
Expand Tier II Rat 570 Genes GS224709: Estrogen induced uterine response QTL 2 (Eutr2 Published QTL Chr 5)
Expand Tier I Mouse GO 13255 Genes GS178461: GO:0009987 cellular process
Expand Tier II Human 8948 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 6611 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Mouse MP 25 Genes GS169482: MP:0001300 ocular hypertelorism
Expand Tier I Mouse GO 3536 Genes GS192041: GO:0043169 cation binding
Expand Tier II Rat 322 Genes GS224349: Blood pressure QTL 293 (Bp293 Published QTL Chr 5)
Expand Tier II Mouse 356 Genes GS135525: body weight QTL 9 (Bwtq9, Published QTL Chr 4)
Expand Tier I Mouse MP 18 Genes GS166522: MP:0005189 abnormal anogenital distance
Expand Tier II Human 602 Genes GS245714: [MeSH] Face : D005145
Expand Tier I Human 841 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 22753 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human CTD 5877 Genes GS121789: (6-(4-(2-piperidin-1-ylethoxy)phenyl))-3-pyridin-4-ylpyrazolo(1,5-a)pyrimidine interacting with Homo sapiens associated genes (MeSH:C516138) in CTD
Expand Tier I Mouse CTD 3927 Genes GS256188: Valinomycin interacting with Mus musculus associated genes (MeSH:D014634) in CTD
Expand Tier I Mouse MP 26 Genes GS163905: MP:0000493 rectal prolapse
Expand Tier I Mouse MP 345 Genes GS166406: MP:0002110 abnormal digit morphology
Expand Tier II Human 9308 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier II Human 34 Genes GS241627: [MeSH] Coloboma : D003103
Expand Tier II Human 4853 Genes GS239764: [MeSH] Glycoproteins : D006023
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier II Mouse 281 Genes GS83989: cocaine related behavior 5 (Cocrb5, Published QTL,Chr 4, MGI:2150991)
Expand Tier I Mouse MP 3 Genes GS162863: MP:0005242 cryptophthalmos
Expand Tier I Human GO 4064 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier II Rat 415 Genes GS224889: Proteinuria QTL 21 (Pur21 Published QTL Chr 5)
Expand Tier II Human 1562 Genes GS245025: [MeSH] Receptors, Cytokine : D018121
Expand Tier I Human 51 Genes GS172891: HP:0100538 Abnormality of the supraorbital ridges
Expand Tier I Human GO 4016 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier II Human 338 Genes GS237845: [MeSH] Bone Diseases, Developmental : D001848
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier II Human 4278 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
Expand Tier I Human 783 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse GO 5732 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 637 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Mouse MP 64 Genes GS169473: MP:0001302 eyelids open at birth
Expand Tier I Human GO 953 Genes GS195976: GO:0007155 cell adhesion
Expand Tier II Mouse 41 Genes GS36706: Neocortex Gene expression correlates of Morphine vertical activity counts minutes 45-60 in Females & Males BXD
Expand Tier I Human 25 Genes GS268952: GWAS Catalog Data for body height in 8,842 Korean ancestry individuals
Expand Tier I Human 10 Genes GS172838: HP:0004122 Midline defect of the nose
Expand Tier I Human 44 Genes GS174484: HP:0000521 Abnormality of tear glands or tear production
Expand Tier II Human 7608 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier I Human GO 95 Genes GS195460: GO:0060348 bone development
Expand Tier I Mouse MP 2295 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 1879 Genes GS165528: MP:0005379 endocrine/exocrine gland phenotype
Expand Tier I Human 122 Genes GS229306: MSigDB Geneset - ACTGTAG,MIR-139
Expand Tier I Mouse MP 37 Genes GS164508: MP:0006000 abnormal corneal epithelium morphology
Expand Tier I Mouse MP 1902 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier II Rat 253 Genes GS223798: Body weight QTL 84 (Bw84 Published QTL Chr 5)
Expand Tier II Human 701 Genes GS238780: [MeSH] Head : D006257
Expand Tier I Mouse MP 16 Genes GS170406: MP:0005543 decreased cornea thickness
Expand Tier II Rat 253 Genes GS224710: Serum cholesterol level QTL 64 (Scl64 Published QTL Chr 5)
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Mouse GO 3076 Genes GS177265: GO:0048731 system development
Expand Tier I Human 1417 Genes GS232484: PC Geneset - "CAGCTG_V$AP4_Q5" pathway genes
Expand Tier II Rat 920 Genes GS224620: Serum cholesterol level QTL 2 (Scl2 Published QTL Chr 5)
Expand Tier I Mouse GO 3592 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 4 Genes GS168317: MP:0004472 broad nasal bone
Expand Tier I Mouse GO 3441 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Mouse MP 549 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1091 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier II Rat 313 Genes GS223481: Mammary carcinoma susceptibility QTL 24 (Mcs24 Published QTL Chr 5)
Expand Tier II Mouse 357 Genes GS135446: bone length and organs 2 (Bod2, Published QTL Chr 4)
Expand Tier I Mouse MP 738 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Human CTD 3339 Genes GS126466: Quercetin interacting with Homo sapiens associated genes (MeSH:D011794) in CTD
Expand Tier II Human 6064 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier II Mouse 376 Genes GS84162: chronic alcohol withdrawal severity (Published QTL, Chr 4)
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier II Rat 785 Genes GS223949: Renal function QTL 33 (Rf33 Published QTL Chr 5)
Expand Tier I Mouse MP 342 Genes GS169176: MP:0000759 abnormal skeletal muscle morphology
Expand Tier I Human CTD 2002 Genes GS123157: Carbamazepine interacting with Homo sapiens associated genes (MeSH:D002220) in CTD
Expand Tier I Mouse MP 243 Genes GS169962: MP:0001286 abnormal eye development
Expand Tier II Human 2173 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier I Human 451 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier II Mouse 296 Genes GS84159: alcohol withdrawal (Published QTL, Chr 4)
Expand Tier II Human 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier I Human 220 Genes GS227537: MSigDB Geneset - AAAGGGA,MIR-204,MIR-211
Expand Tier II Human 1876 Genes GS240837: [MeSH] Polysaccharides : D011134
Expand Tier II Rat 415 Genes GS224775: Food consumption QTL 3 (Foco3 Published QTL Chr 5)
Expand Tier I Mouse MP 12 Genes GS166243: MP:0000081 premature suture closure
Expand Tier I Mouse GO 822 Genes GS183355: GO:0022610 biological adhesion
Expand Tier I Mouse CTD 6607 Genes GS257260: Vehicle Emissions interacting with Mus musculus associated genes (MeSH:D001335) in CTD
Expand Tier II Rat 1235 Genes GS224291: Serum cholesterol level QTL 44 (Scl44 Published QTL Chr 5)
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Mouse MP 12 Genes GS167958: MP:0001341 absent eyelids
Expand Tier I Human CTD 5877 Genes GS126658: 2,3-dimethylhydroquinone interacting with Homo sapiens associated genes (MeSH:C516077) in CTD
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Human GO 4009 Genes GS208978: GO:0043169 cation binding
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Mouse MP 27 Genes GS169681: MP:0010975 abnormal lung lobe morphology
Expand Tier II Human 10126 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human CTD 1304 Genes GS123789: panobinostat interacting with Homo sapiens associated genes (MeSH:C496932) in CTD
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse GO 758 Genes GS188757: GO:0009887 organ morphogenesis
Expand Tier II Human 188 Genes GS243315: [MeSH] Non-Fibrillar Collagens : D024041
Expand Tier II Human 1454 Genes GS238126: [MeSH] Integumentary System : D034582
Expand Tier I Human 48 Genes GS173103: HP:0004378 Abnormality of the anus
Expand Tier II Human 3665 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 125 Genes GS230660: MSigDB Geneset - CCTGTGA,MIR-513
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier I Human 402 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier II Human 11248 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier II Mouse 328 Genes GS129092: bone mechanical trait 2 (Bmch2 Published QTL Chr 4)
Expand Tier I Mouse MP 1251 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier II Rat 1091 Genes GS223356: Alcohol response QTL 18 (Alcrsp18 Published QTL Chr 5)
Expand Tier II Human 1477 Genes GS242312: [MeSH] Extracellular Matrix Proteins : D016326
Expand Tier II Mouse 297 Genes GS136495: proteoglycan induced arthritis 27 (Pgia27, Published QTL Chr 4)
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 126 Genes GS239135: [MeSH] Digestive System Abnormalities : D004065
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 32 Genes GS172787: HP:0001539 Omphalocele
Expand Tier II Human 812 Genes GS238243: [MeSH] Bone Diseases : D001847
Expand Tier II Human 332 Genes GS237939: [MeSH] Chromosomes, Human, Pair 9 : D002899
Expand Tier II Human 7632 Genes GS236362: [MeSH] Organic Chemistry Phenomena : D055601
Expand Tier I Human GO 5627 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier II Mouse 459 Genes GS129186: silicosis susceptibility 1 (Slcs1 Published QTL Chr 4)
Expand Tier II Human 7529 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Mouse GO 9 Genes GS183446: GO:0097094 craniofacial suture morphogenesis
Expand Tier II Mouse 359 Genes GS135467: blood pressure QTL 3 (Bpq3, Published QTL Chr 4)
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Mouse 361 Genes GS135541: cerebellar cAMP 4 (Ccmp4, Published QTL Chr 4)
Expand Tier II Mouse 272 Genes GS136419: plasma apolipoprotein B (human) regulator 2 (Pabr2, Published QTL Chr 4)
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Mouse MP 1069 Genes GS169832: MP:0005381 digestive/alimentary phenotype
Expand Tier I Mouse GO 121 Genes GS182054: GO:0007160 cell-matrix adhesion
Expand Tier II Human 2769 Genes GS239065: [MeSH] Urinary Tract : D014551
Expand Tier I Mouse MP 59 Genes GS170233: MP:0001299 abnormal eye distance/ position
Expand Tier II Human 706 Genes GS234536: [MeSH] Receptors, Interleukin : D018123
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 185 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier II Human 10556 Genes GS235415: [MeSH] Embryo, Mammalian : D004622
Expand Tier I Mouse MP 8 Genes GS164068: MP:0008854 bleb
Expand Tier I Human CTD 660 Genes GS124847: belinostat interacting with Homo sapiens associated genes (MeSH:C487081) in CTD
Expand Tier I Mouse MP 652 Genes GS166407: MP:0002116 abnormal craniofacial bone morphology
Expand Tier I Mouse GO 22332 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Rat 332 Genes GS224958: Kidney mass QTL 25 (Kidm25 Published QTL Chr 5)
Expand Tier I Human GO 5251 Genes GS207615: GO:0016021 integral to membrane
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Mouse 541 Genes GS136760: soft tissue heal 4 (Stheal4, Published QTL Chr 4)
Expand Tier I Human CTD 3952 Genes GS126200: Nickel interacting with Homo sapiens associated genes (MeSH:D009532) in CTD
Expand Tier I Mouse MP 417 Genes GS164665: MP:0000572 abnormal autopod morphology
Expand Tier II Human 18556 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Mouse MP 35 Genes GS163402: MP:0005262 coloboma
Expand Tier II Human 1245 Genes GS235642: [MeSH] Body Regions : D001829
Expand Tier I Mouse GO 5224 Genes GS189860: GO:0043167 ion binding
Expand Tier II Rat 415 Genes GS224698: Body weight QTL 135 (Bw135 Published QTL Chr 5)
Expand Tier I Mouse GO 1465 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 402 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse CTD 3927 Genes GS256187: Valproic Acid interacting with Mus musculus associated genes (MeSH:D014635) in CTD
Expand Tier II Human 17 Genes GS245690: [MeSH] Anal Canal : D001003
Expand Tier I Mouse CTD 7038 Genes GS255863: Nanotubes, Carbon interacting with Mus musculus associated genes (MeSH:D037742) in CTD
Expand Tier I Mouse GO 6471 Genes GS184448: GO:0044425 membrane part
Expand Tier II Human 7440 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Mouse 299 Genes GS136700: systemic lupus erythmatosus susceptibility 2 (Sle2, Published QTL Chr 4)
Expand Tier I Mouse MP 648 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier II Human 15970 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Mouse MP 115 Genes GS170033: MP:0003358 abnormal hypaxial muscle morphology
Expand Tier I Mouse MP 697 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse MP 813 Genes GS166118: MP:0002109 abnormal limb morphology
Expand Tier II Human 2806 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier II Human 257 Genes GS240120: [MeSH] Basement Membrane : D001485
Expand Tier II Mouse 282 Genes GS136485: predicted fat percentage 1 (Pfat1, Published QTL Chr 4)
Expand Tier I Mouse MP 206 Genes GS167970: MP:0001340 abnormal eyelid morphology
Expand Tier II Human 3351 Genes GS244779: [MeSH] Embryonic and Fetal Development : D005314
Expand Tier II Human 6 Genes GS245217: [MeSH] Hypertelorism : D006972
Expand Tier II Mouse 287 Genes GS84160: METH responses for climbing Ms6hm (Published QTL, Chr 4)
Expand Tier I Mouse MP 2915 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier II Human 13379 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Human 2330 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Human 14 Genes GS239326: [MeSH] Craniofacial Dysostosis : D003394
Expand Tier II Human 1304 Genes GS240993: [MeSH] Intestines : D007422
Expand Tier I Human GO 177 Genes GS202566: GO:0048705 skeletal system morphogenesis
Expand Tier I Human GO 5774 Genes GS206742: GO:0043167 ion binding
Expand Tier II Mouse 361 Genes GS136116: body length 3 (Lgth3, Published QTL Chr 4)
Expand Tier II Mouse 280 Genes GS136776: synechia 2 (Synch2, Published QTL Chr 4)
Expand Tier II Rat 370 Genes GS224985: Blood pressure QTL 156 (Bp156 Published QTL Chr 5)
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier II Rat 653 Genes GS224956: CIA Autoantibody QTL 5 (Ciaa5 Published QTL Chr 5)
Expand Tier I Mouse MP 1780 Genes GS166590: MP:0002873 normal phenotype
Expand Tier I Human CTD 1267 Genes GS123763: Testolactone interacting with Homo sapiens associated genes (MeSH:D013738) in CTD
Expand Tier I Mouse MP 1027 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier I Human CTD 31 Genes GS123042: indeno(1,2,3-cd)pyrene interacting with Homo sapiens associated genes (MeSH:C041508) in CTD
Expand Tier I Mouse GO 338 Genes GS190605: GO:0001501 skeletal system development
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier II Mouse 357 Genes GS136231: mandible length 5 (Manln5, Published QTL Chr 4)
Expand Tier I Mouse MP 37 Genes GS163904: MP:0000492 abnormal rectum morphology
Expand Tier II Human 9339 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier I Human 46 Genes GS173611: HP:0002219 Facial hypertrichosis
Expand Tier II Human 9390 Genes GS235446: [MeSH] Reproductive and Urinary Physiological Phenomena : D012101
Expand Tier I Human 12 Genes GS175927: HP:0000243 Trigonocephaly
Expand Tier II Human 11557 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier I Human CTD 3934 Genes GS126584: Tetrachlorodibenzodioxin interacting with Oryzias latipes associated genes (MeSH:D013749) in CTD
Expand Tier I Mouse MP 11 Genes GS167517: MP:0001310 abnormal conjunctiva morphology
Expand Tier II Rat 678 Genes GS224253: Estrogen-induced mammary cancer QTL 13 (Emca13 Published QTL Chr 5)
Expand Tier II Human 222 Genes GS241075: [MeSH] Myeloid Differentiation Factor 88 : D053594
Expand Tier II Human 5300 Genes GS234570: [MeSH] Cell Differentiation : D002454
Expand Tier I Mouse MP 1471 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier II Mouse 347 Genes GS129083: atherosclerosis 8 (Ath8 Published QTL Chr 4)
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1069 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier II Human 10111 Genes GS235272: [MeSH] Membrane Proteins : D008565
Expand Tier II Human 335 Genes GS235950: [MeSH] Hair Follicle : D018859
Expand Tier I Mouse GO 10875 Genes GS181473: GO:0005488 binding
Expand Tier II Human 10 Genes GS235963: [MeSH] Collagen Type VII : D024143
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier II Mouse 543 Genes GS129184: skin tumor susceptibility in FVB and PWK 1 (Skts-fp1 Published QTL Chr 4)
Expand Tier I Mouse GO 5884 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 61 Genes GS168361: MP:0000102 abnormal nasal bone morphology
Expand Tier I Mouse MP 689 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier II Rat 253 Genes GS223929: Body weight QTL 44 (Bw44 Published QTL Chr 5)
Expand Tier I Mouse MP 640 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse GO 8142 Genes GS190714: GO:0016020 membrane
Expand Tier II Human 7335 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier II Human 14403 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier II Human 4 Genes GS239688: [MeSH] Anus, Imperforate : D001006
Expand Tier I Human 584 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7725 Genes GS207616: GO:0016020 membrane
Expand Tier I Mouse MP 22 Genes GS166620: MP:0003416 premature bone ossification
Expand Tier II Human 4886 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier I Human GO 12781 Genes GS195214: GO:0009987 cellular process
Expand Tier II Mouse 272 Genes GS136358: NOD Sjogren's syndrome 1 (Nss1, Published QTL Chr 4)
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse GO 4068 Genes GS180034: GO:0032502 developmental process
Expand Tier II Rat 424 Genes GS223186: Body weight QTL 113 (Bw113 Published QTL Chr 5)
Expand Tier I Human CTD 1044 Genes GS254642: mercuric bromide interacting with Homo sapiens associated genes (MeSH:C042720) in CTD
Expand Tier I Mouse MP 834 Genes GS169389: MP:0002060 abnormal skin morphology
Expand Tier II Mouse 442 Genes GS136936: vertebral trabecular bone trait 3 (Vtbt3, Published QTL Chr 4)
Expand Tier II Rat 332 Genes GS223936: Blood pressure QTL 261 (Bp261 Published QTL Chr 5)
Expand Tier I Mouse MP 4704 Genes GS165525: MP:0010768 mortality/aging
Expand Tier II Human 14645 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 12777 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Mouse 357 Genes GS135409: body growth late QTL 4 (Bglq4, Published QTL Chr 4)
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Human 8 Genes GS176456: HP:0001545 Anteriorly placed anus
Expand Tier I Human GO 216 Genes GS195701: GO:0031589 cell-substrate adhesion
Expand Tier II Mouse 306 Genes GS136516: plasma lepin levels (Plep, Published QTL Chr 4)
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier II Human 356 Genes GS238444: [MeSH] Nose : D009666
Expand Tier II Mouse 459 Genes GS129177: splenomegaly-NZB x NZW 2 (Sbw2 Published QTL Chr 4)
Expand Tier I Mouse MP 2874 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 909 Genes GS165869: MP:0002138 abnormal hepatobiliary system morphology
Expand Tier II Mouse 382 Genes GS135357: B.burgdorferi-associated arthritis 1 (Bbaa1, Published QTL Chr 4)
Expand Tier I Human CTD 4501 Genes GS125634: trichostatin A interacting with Homo sapiens associated genes (MeSH:C012589) in CTD
Expand Tier II Rat 986 Genes GS223510: Serum renin concentration QTL 6 (Srn6 Published QTL Chr 5)
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 756 Genes GS240201: [MeSH] Epidermis : D004817
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier II Mouse 459 Genes GS129191: seizure susceptibility 2 (Szs2 Published QTL Chr 4)
Expand Tier I Human 419 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3507 Genes GS193991: GO:0048731 system development
Expand Tier II Human 500 Genes GS241756: [MeSH] Craniofacial Abnormalities : D019465
Expand Tier II Human 8835 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier II Mouse 476 Genes GS136422: pulmonary adenoma progression 1 (Papg1, Published QTL Chr 4)
Expand Tier I Mouse MP 51 Genes GS166611: MP:0002835 abnormal cranial suture morphology
Expand Tier II Human 803 Genes GS236430: [MeSH] Integrins : D016023
Expand Tier I Human 310 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier II Mouse 311 Genes GS136247: metabolic syndrome (Mbsyd, Published QTL Chr 4)
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human GO 11880 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse GO 1040 Genes GS184451: GO:0044421 extracellular region part
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier II Mouse 116 Genes GS35614: Neocortex Gene expression correlates of Morphine photocell counts minutes 15-30 in Males BXD
Expand Tier II Rat 1117 Genes GS224126: Non-insulin dependent diabetes mellitus QTL 25 (Niddm25 Published QTL Chr 5)
Expand Tier I Human CTD 57 Genes GS125463: benz(a)anthracene interacting with Homo sapiens associated genes (MeSH:C030935) in CTD
Expand Tier II Human 11230 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 14014 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier II Human 7110 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier II Human 3173 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Human CTD 1267 Genes GS123759: Testosterone interacting with Homo sapiens associated genes (MeSH:D013739) in CTD
Expand Tier I Mouse MP 3960 Genes GS165527: MP:0005378 growth/size/body region phenotype
Expand Tier I Mouse GO 1823 Genes GS193270: GO:0005576 extracellular region
Expand Tier II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Mouse MP 39 Genes GS163414: MP:0009570 abnormal right lung morphology
Expand Tier I Human 15 Genes GS175229: HP:0002025 Anal stenosis
Expand Tier II Human 9704 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 196 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Mouse MP 4387 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Mouse MP 7 Genes GS169949: MP:0003842 abnormal metopic suture morphology
Expand Tier II Rat 599 Genes GS223791: Blood pressure QTL 254 (Bp254 Published QTL Chr 5)
Expand Tier II Human 661 Genes GS238687: [MeSH] Disease : D004194
Expand Tier I Human GO 3909 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Mouse CTD 172 Genes GS256924: Ethylnitrosourea interacting with Mus musculus associated genes (MeSH:D005038) in CTD
Expand Tier II Human 3864 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier I Mouse MP 26 Genes GS167904: MP:0003924 diaphragmatic hernia
Expand Tier II Human 1643 Genes GS239636: [MeSH] Cell Adhesion : D002448
Expand Tier I Human 168 Genes GS230761: MSigDB Geneset - GSE17974_IL4_AND_ANTI_IL12_VS_UNTREATED_1H_ACT_CD4_TCELL_UP
Expand Tier II Human 646 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 4699 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human CTD 5902 Genes GS124700: 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide interacting with Homo sapiens associated genes (MeSH:C459179) in CTD
Expand Tier II Mouse 476 Genes GS136173: lens opacity 1 (Lnopy1, Published QTL Chr 4)
Expand Tier I Mouse MP 481 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse MP 3894 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier II Human 2729 Genes GS243574: [MeSH] Kidney : D007668
Expand Tier I Human 357 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier II Human 5703 Genes GS235196: [MeSH] Phosphorylation : D010766
Expand Tier II Human 5577 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier II Human 847 Genes GS241252: [MeSH] Collagen : D003094
Expand Tier I Mouse GO 95 Genes GS178703: GO:0060348 bone development
Expand Tier II Rat 731 Genes GS223574: Thyroid stimulating hormone level QTL 2 (Thshl2 Published QTL Chr 5)
Expand Tier II Mouse 357 Genes GS136237: mandible size 3 (Manz3, Published QTL Chr 4)
Expand Tier II Human 10961 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Mouse GO 68 Genes GS178702: GO:0060349 bone morphogenesis
Expand Tier I Mouse MP 46 Genes GS165971: MP:0008273 abnormal intramembranous bone ossification
Expand Tier I Human 19 Genes GS173649: HP:0004397 Ectopic anus
Expand Tier II Human 1665 Genes GS239484: [MeSH] Gastrointestinal Tract : D041981
Expand Tier II Mouse 307 Genes GS136845: thymic lymphoma suppressor region 4 (Tlsr4, Published QTL Chr 4)
Expand Tier I Mouse MP 987 Genes GS165798: MP:0005367 renal/urinary system phenotype
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier II Human 549 Genes GS245859: [MeSH] Proteoglycans : D011509
Expand Tier I Human GO 2540 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 1047 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 8777 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Human CTD 7249 Genes GS123768: Cyclosporine interacting with Homo sapiens associated genes (MeSH:D016572) in CTD
Expand Tier II Human 3688 Genes GS241772: [MeSH] Carbohydrates : D002241
Expand Tier I Human CTD 3043 Genes GS251470: Phenylmercuric Acetate interacting with Homo sapiens associated genes (MeSH:D010662) in CTD
Expand Tier II Rat 297 Genes GS224313: Blood pressure QTL 49 (Bp49 Published QTL Chr 5)
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier II Rat 253 Genes GS224146: Estrogen-dependent pituitary mass QTL 5 (Edpm5 Published QTL Chr 5)
Expand Tier II Human 5184 Genes GS241851: [MeSH] Receptors, Cell Surface : D011956
Expand Tier I Mouse MP 319 Genes GS164004: MP:0011101 prenatal lethality, incomplete penetrance
Expand Tier I Mouse MP 639 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier II Human 1432 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Mouse MP 101 Genes GS170238: MP:0001293 anophthalmia
Expand Tier II Rat 1467 Genes GS224712: Tongue tumor susceptibility QTL 11 (Tcas11 Published QTL Chr 5)
Expand Tier I Human GO 1586 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Mouse MP 114 Genes GS164685: MP:0000564 syndactyly
Expand Tier I Mouse MP 265 Genes GS169017: MP:0002932 abnormal joint morphology
Expand Tier I Mouse GO 1849 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 470 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human CTD 4423 Genes GS123048: Tretinoin interacting with Homo sapiens associated genes (MeSH:D014212) in CTD
Expand Tier II Mouse 359 Genes GS136067: immune response to AAV2 QTL 1 (Imraq1, Published QTL Chr 4)
Expand Tier I Human GO 268 Genes GS196679: GO:0030246 carbohydrate binding
Expand Tier II Human 1748 Genes GS243170: [MeSH] Respiratory System : D012137
Expand Tier I Human GO 6081 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 27 Genes GS171447: HP:0000601 Hypotelorism
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 14 Genes GS171660: HP:0000614 Abnormality of the nasolacrimal system
Expand Tier I Human GO 66 Genes GS195459: GO:0060349 bone morphogenesis
Expand Tier I Mouse MP 2172 Genes GS164262: MP:0002080 prenatal lethality
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Mouse MP 20 Genes GS168990: MP:0005084 abnormal gallbladder morphology
Expand Tier II Rat 1182 Genes GS224560: Serum cholesterol level QTL 20 (Scl20 Published QTL Chr 5)
Expand Tier II Human 2741 Genes GS237173: [MeSH] Digestive System Diseases : D004066
Expand Tier II Mouse 299 Genes GS135504: bulb size 1 (Bulb1, Published QTL Chr 4)
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Mouse 361 Genes GS136182: lymphoproliferation modifier 1 (Lprm1, Published QTL Chr 4)
Expand Tier II Rat 897 Genes GS224433: Serum cholesterol level QTL 54 (Scl54 Published QTL Chr 5)
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier I Human 565 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human CTD 10572 Genes GS125506: Valproic Acid interacting with Homo sapiens associated genes (MeSH:D014635) in CTD
Expand Tier II Human 3057 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier II Mouse 104 Genes GS35629: Neocortex Gene expression correlates of Morphine photocell counts minutes 30-45 in Males BXD
Expand Tier I Mouse GO 815 Genes GS179210: GO:0007155 cell adhesion
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier II Mouse 440 Genes GS135242: anti-dsDNA antibody production in NZM 1 (Adaz1, Published QTL Chr 4)
Expand Tier II Human 11279 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier II Mouse 287 Genes GS84161: high-dose ethanol actions (Published QTL, Chr 4)
Expand Tier I Human GO 11 Genes GS200240: GO:0097094 craniofacial suture morphogenesis
Expand Tier II Human 7589 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier I Mouse MP 404 Genes GS166194: MP:0009931 abnormal skin appearance
Expand Tier I Mouse MP 432 Genes GS168088: MP:0011110 preweaning lethality, incomplete penetrance
Expand Tier II Human 9375 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Human 1206 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 4554 Genes GS241940: [MeSH] Urogenital System : D014566
Expand Tier II Human 1402 Genes GS237932: [MeSH] Skin : D012867
Expand Tier II Human 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Mouse MP 208 Genes GS170240: MP:0001297 microphthalmia
Expand Tier I Mouse MP 1210 Genes GS166711: MP:0002160 abnormal reproductive system morphology
Expand Tier I Mouse MP 1961 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human 71 Genes GS174898: HP:0100887 Abnormality of globe size
Expand Tier II Rat 774 Genes GS224164: Mammary tumor resistance QTL 1 (Mamtr1 Published QTL Chr 5)
Expand Tier II Human 6771 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Mouse MP 1143 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse MP 24 Genes GS163489: MP:0001208 blistering
Expand Tier I Human 17 Genes GS172814: HP:0000336 Prominent supraorbital ridges
Expand Tier II Human 2422 Genes GS240538: [MeSH] Embryonic Development : D047108
Expand Tier I Mouse MP 480 Genes GS167563: MP:0001175 abnormal lung morphology
Expand Tier I Human GO 5367 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 408 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human CTD 2385 Genes GS126764: Calcitriol interacting with Homo sapiens associated genes (MeSH:D002117) in CTD
Expand Tier I Mouse MP 75 Genes GS169785: MP:0000733 abnormal muscle development
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 89 Genes GS208328: GO:0005604 basement membrane
Expand Tier II Mouse 419 Genes GS136743: splenomegaly modifier (Spm1, Published QTL Chr 4)
Expand Tier I Mouse MP 2061 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier II Human 9890 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Mouse GO 94 Genes GS191405: GO:0005604 basement membrane
Expand Tier II Rat 809 Genes GS223458: Mammary carcinoma susceptibility QTL 5 (Mcs5 Published QTL Chr 5)
Expand Tier I Mouse MP 158 Genes GS164411: MP:0000562 polydactyly
Expand Tier II Human 1449 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier I Mouse MP 1717 Genes GS166710: MP:0002163 abnormal gland morphology
Expand Tier I Human 10 Genes GS175118: HP:0000579 Nasolacrimal duct obstruction
Expand Tier I Mouse MP 12 Genes GS169556: MP:0003418 premature intramembranous bone ossification
Expand Tier II Rat 473 Genes GS224526: T-lymphoma susceptibility QTL 1 (Tls1 Published QTL Chr 5)
Expand Tier II Mouse 440 Genes GS136036: induction of brown adipocytes 7 (Iba7, Published QTL Chr 4)
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier II Mouse 476 Genes GS135879: femur geometry 3 (Fmgty3, Published QTL Chr 4)
Expand Tier II Rat 253 Genes GS223938: Body weight QTL 46 (Bw46 Published QTL Chr 5)
Expand Tier I Mouse MP 1870 Genes GS165244: MP:0010771 integument phenotype
Expand Tier II Mouse 883 Genes GS129123: cataract severity (Ctrcts Published QTL Chr 4)
Expand Tier II Mouse 541 Genes GS136003: hepatocarcinogen resistance 1 (Hpcr1, Published QTL Chr 4)
Expand Tier I Human 11971 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Human 937 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14517 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse MP 191 Genes GS167518: MP:0001312 abnormal cornea morphology
Expand Tier I Human 44 Genes GS229315: MSigDB Geneset - chr9p22
Expand Tier I Mouse MP 343 Genes GS165567: MP:0008271 abnormal bone ossification
Expand Tier II Rat 1295 Genes GS224319: Blood pressure QTL 7 (Bp7 Published QTL Chr 5)
Expand Tier II Human 420 Genes GS234441: [MeSH] Hair : D006197
Expand Tier II Human 229 Genes GS237839: [MeSH] Eye Abnormalities : D005124
Expand Tier I Mouse MP 11231 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 753 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier II Human 9296 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier I Mouse MP 2 Genes GS163823: MP:0008862 asymmetric snout
Expand Tier II Human 7086 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse MP 454 Genes GS163664: MP:0005274 abnormal viscerocranium morphology
Expand Tier I Mouse GO 194 Genes GS178944: GO:0031589 cell-substrate adhesion
Expand Tier I Human GO 791 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Mouse MP 100 Genes GS167316: MP:0003942 abnormal urinary system development
Expand Tier I Human 522 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Mouse MP 5 Genes GS168054: MP:0010977 fused right lung lobes
Expand Tier I Human 1099 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Mouse 396 Genes GS84158: cocaine related behavior (Published QTL, Cocrb5, Chr 4)
Expand Tier II Human 9373 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier I Mouse GO 219 Genes GS179910: GO:0030246 carbohydrate binding
Expand Tier II Human 14808 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Mouse MP 727 Genes GS165875: MP:0002132 abnormal respiratory system morphology
Expand Tier I Mouse GO 5871 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Mouse GO 3601 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier II Mouse 480 Genes GS135309: anxiety (Anxty, Published QTL Chr 4)
Expand Tier I Human GO 955 Genes GS200151: GO:0022610 biological adhesion
Expand Tier II Mouse 382 Genes GS135443: bone marrow graft rejection 4 (Bmgr4, Published QTL Chr 4)
Expand Tier I Mouse MP 24 Genes GS165734: MP:0005176 eyelids fail to open
Expand Tier II Human 3949 Genes GS240624: [MeSH] Adaptor Proteins, Signal Transducing : D048868
Expand Tier I Human 12 Genes GS175372: HP:0011481 Abnormality of the lacrimal duct
Expand Tier I Human GO 1093 Genes GS201255: GO:0044421 extracellular region part
Expand Tier II Mouse 361 Genes GS135888: free running period 1 (Frp1, Published QTL Chr 4)
Expand Tier I Mouse MP 51 Genes GS168994: MP:0005083 abnormal biliary tract morphology
Expand Tier II Mouse 476 Genes GS135364: B.burgdorferi-associated arthritis 23 (Bbaa23, Published QTL Chr 4)
Expand Tier I Mouse MP 834 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier II Human 151